Nanotechnology approach for drug addiction therapy: Gene silencing using delivery of gold nanorod-siRNA nanoplex in dopaminergic neurons

被引:158
作者
Bonoiu, Adela C. [1 ]
Mahajan, Supriya D. [2 ]
Ding, Hong [1 ]
Roy, Indrajit [1 ]
Yong, Ken-Tye [1 ]
Kumar, Rajiv [1 ]
Hu, Rui [1 ]
Bergey, Earl J. [1 ]
Schwartz, Stanley A. [2 ]
Prasad, Paras N. [1 ]
机构
[1] SUNY Buffalo, Inst Lasers Photon & Biophoton, Buffalo, NY 14260 USA
[2] SUNY Buffalo, Dept Med, Div Rheumatol Allergy & Immunol, Buffalo Gen Hosp, Buffalo, NY 14203 USA
关键词
DARPP-32; dark field imaging; surface plasmon resonance; nanoplexes; blood-brain barrier; BLOOD-BRAIN-BARRIER; PHOSPHATASE-1; CASCADE; HIV-1; ENCEPHALITIS; NANOPARTICLES; DARPP-32; PERMEABILITY; MODELS; ABUSE; THERAPEUTICS; PLASTICITY;
D O I
10.1073/pnas.0901715106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Drug abuse is a worldwide health concern in which addiction involves activation of the dopaminergic signaling pathway in the brain. Here, we introduce a nanotechnology approach that utilizes gold nanorod-DARPP-32 siRNA complexes (nanoplexes) that target this dopaminergic signaling pathway in the brain. The shift in the localized longitudinal plasmon resonance peak of gold nanorods (GNRs) was used to show their interaction with siRNA. Plasmonic enhanced dark field imaging was used to visualize the uptake of these nanoplexes in dopaminergic neurons in vitro. Gene silencing of the nanoplexes in these cells was evidenced by the reduction in the expression of key proteins (DARPP-32, ERK, and PP-1) belonging to this pathway, with no observed cytotoxicity. Moreover, these nanoplexes were shown to transmigrate across an in vitro model of the blood-brain barrier (BBB). Therefore, these nanoplexes appear to be suited for brain-specific delivery of appropriate siRNA for therapy of drug addiction and other brain diseases.
引用
收藏
页码:5546 / 5550
页数:5
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